A Pilot Randomized Controlled Trial of MRI-guided Focused Low-intensity Transcranial Ultrasound Stimulation (TUS) for Sleep Disturbances in Patients With Chronic Tinnitus

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Background: Tinnitus, as a common symptom, can jeopardize the sleep quality and brain function and even lead to hearing loss and cognitive decline in elderly patients. The co-occurring tinnitus and sleep disturbances can significantly affect the cognitive functions and quality of life, and even be implicated as a key contributing factor in the development of prodromal dementia. At present, very few non-pharmacological therapies are developed for managing these comorbidities in elderly patients. Focused low-intensity transcranial ultrasound stimulation (TUS) enables to stimulation the deep brain structures, such as hippocampus, with optimized focality and specific frequency.

Objectives: We aim to 1) investigate the safety, feasibility and efficacy of a 2-week focused low-intensity TUS on the severity of tinnitus and sleep disturbances in elderly patients; 2) determine the sample size of a full-scale randomized clinical trial of low-intensity TUS in patients with tinnitus; 3) evaluate the effects of low-intensity TUS on the severity of tinnitus, sleep quality and cognitive functions at 2, 4 and 6 weeks after the treatments.

Design: A 2-week randomized, double-blind, controlled clinical trial.

Methods: Chinese right-handed tinnitus patients with sleep disturbances (aged from 60 to 90 years) will be randomly assigned to a 2-week intervention of either low intensity TUS or sham TUS, with 7 participants per arm. Before intervention, T1-weighted magnetic resonance imaging (MRI) and diffusion-weighted imaging (DWI) data is used to construct individual realistic head model. Comprehensive assessments, including sleep quality, cognitive performance and quality of life will be conducted at baseline, 2nd week, 4th week and 6th week. Program adherence and adverse effects will be monitored throughout intervention.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 60
Maximum Age: 85
Healthy Volunteers: f
View:

• Chinese, right-handed, aged from 60 to 80 years.

• Chronic tinnitus is defined as tinnitus with a duration of at least 3 months. Depending on the justification, different time course definitions of chronic tinnitus are possible.

• Sleep disturbances are defined as a Pittsburgh Sleep Quality Index (PSQI) total score above 5.

• No interference with independence in everyday activities.

Locations
Other Locations
Hong Kong Special Administrative Region
Tai Po Hospital
NOT_YET_RECRUITING
Hong Kong
Tai Po Hospital
RECRUITING
Hong Kong
Contact Information
Primary
Xi Ni, PhD
xini@cuhk.edu.hk
852-28314305
Time Frame
Start Date: 2025-01-15
Estimated Completion Date: 2026-06-30
Participants
Target number of participants: 14
Treatments
Active_comparator: Active TUS
In active TUS group, participants will receive 500 kHz low-intensity TUS.
Sham_comparator: Sham TUS
In sham TUS group, participants will not receive low-intensity TUS.
Sponsors
Leads: Chinese University of Hong Kong

This content was sourced from clinicaltrials.gov